CVS Health Redness Relief Eye Drops Recalled for Sterility Concerns
Altaire Pharmaceuticals is recalling CVS Health Redness Relief Eye Drops due to a lack of assurance of sterility. Consumers should stop using the product.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a lack of assurance of sterility in a medical product, which poses a significant risk of infection or injury.
Plain-English summary
Altaire Pharmaceuticals, Inc. is recalling CVS Health Redness Relief Lubricant Redness Reliever Eye Drops, Sterile, 1 fl. oz. (30 mL). The product is distributed by CVS Pharmacy Inc. The recall is being conducted because of a lack of assurance of sterility.
The affected lots are 18229 9/21 and 19056 03/22. The product was distributed nationwide in the United States.
Consumers should stop using the recalled eye drops and contact CVS Pharmacy Inc. or Altaire Pharmaceuticals, Inc. for further instructions or a refund.
The recalled product
- Product
- CVS Health Redness Relief Lubricant Redness Reliever Eye Drops, Sterile, 1 fl. oz., (30 mL), Distributed by: CVS Pharmacy Inc., One CVS Drive, Woonsocket, RI 02895
- Manufacturer
- Altaire Pharmaceuticals, Inc.
- Category
- Drug — Ophthalmic
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot #: 18229 9/21 18229 9/21 19056 03/22
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 134 recalled by Altaire Pharmaceuticals, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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